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ES2148476T3 - DERIVATIVES OF AZABICICLOALCANO N-SUBSTITUTED AS NEUROLEPTICOS ASF. - Google Patents

DERIVATIVES OF AZABICICLOALCANO N-SUBSTITUTED AS NEUROLEPTICOS ASF.

Info

Publication number
ES2148476T3
ES2148476T3 ES95903284T ES95903284T ES2148476T3 ES 2148476 T3 ES2148476 T3 ES 2148476T3 ES 95903284 T ES95903284 T ES 95903284T ES 95903284 T ES95903284 T ES 95903284T ES 2148476 T3 ES2148476 T3 ES 2148476T3
Authority
ES
Spain
Prior art keywords
neurolepticos
azabicicloalcano
asf
derivatives
substituted
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES95903284T
Other languages
Spanish (es)
Inventor
Gerd Steiner
Rainer Munschauer
Liliane Unger
Hans-Jurgen Teschendorf
Thomas Hoger
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Application granted granted Critical
Publication of ES2148476T3 publication Critical patent/ES2148476T3/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • A61P21/02Muscle relaxants, e.g. for tetanus or cramps
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/26Psychostimulants, e.g. nicotine, cocaine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D497/00Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D497/02Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D497/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Anesthesiology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Indole Compounds (AREA)
  • Ink Jet (AREA)

Abstract

SE DESCRIBEN COMPUESTO DE FORMULA (I) DONDE B, R 1 , R{SUP,2}, N Y A TIENE LA SIGNIFICACION DADA EN LA DESCRIPCION, Y SU PREPARACION. LOS NUEVOS COMPUESTOS SON APROPIADOS PARA EL CONTROL DE ENFERMEDADES.IT IS DESCRIBED COMPOSED OF FORMULA (I) WHERE B, R 1, R {SUP, 2}, N AND A HAS THE MEANING GIVEN IN THE DESCRIPTION, AND ITS PREPARATION. THE NEW COMPOUNDS ARE SUITABLE FOR DISEASE CONTROL.

ES95903284T 1993-12-04 1994-11-26 DERIVATIVES OF AZABICICLOALCANO N-SUBSTITUTED AS NEUROLEPTICOS ASF. Expired - Lifetime ES2148476T3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4341403A DE4341403A1 (en) 1993-12-04 1993-12-04 N-substituted 3-azabicycloalkane derivatives, their preparation and use

Publications (1)

Publication Number Publication Date
ES2148476T3 true ES2148476T3 (en) 2000-10-16

Family

ID=6504205

Family Applications (1)

Application Number Title Priority Date Filing Date
ES95903284T Expired - Lifetime ES2148476T3 (en) 1993-12-04 1994-11-26 DERIVATIVES OF AZABICICLOALCANO N-SUBSTITUTED AS NEUROLEPTICOS ASF.

Country Status (13)

Country Link
US (1) US5703091A (en)
EP (1) EP0731802B1 (en)
JP (1) JP3935201B2 (en)
AT (1) ATE194620T1 (en)
AU (1) AU680583B2 (en)
BR (1) BR9408246A (en)
DE (2) DE4341403A1 (en)
ES (1) ES2148476T3 (en)
FI (1) FI113644B (en)
IL (1) IL111861A (en)
NO (1) NO306346B1 (en)
TW (1) TW285667B (en)
WO (1) WO1995015327A1 (en)

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DE19848521A1 (en) * 1998-10-21 2000-04-27 Basf Ag Preparation of (+)-exo-6-phenyl-3-azabicyclo(3.2.0)heptane derivatives comprises photocyclization of bisallyl ammonium salts, isomer resolution using (-)-ditoluoyltartaric acid and crystallization
DE19854147A1 (en) * 1998-11-24 2000-05-25 Basf Ag Control of cocaine addiction comprises administration of N-substituted azabicycloalkane derivative
TWI244481B (en) 1998-12-23 2005-12-01 Pfizer 3-azabicyclo[3.1.0]hexane derivatives useful in therapy
GB9912413D0 (en) 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912410D0 (en) 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912417D0 (en) 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912411D0 (en) 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912416D0 (en) 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912415D0 (en) 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
CA2386049A1 (en) 1999-10-15 2001-04-26 Daniel S. Gardner Bicyclic and tricyclic amines as modulators of chemokine receptor activity
US6784200B2 (en) * 2000-10-13 2004-08-31 Bristol-Myers Squibb Pharma Company Bicyclic and tricyclic amines as modulators of chemokine receptor activity
GB0015562D0 (en) * 2000-06-23 2000-08-16 Pfizer Ltd Heterocycles
SE0100326D0 (en) 2001-02-02 2001-02-02 Astrazeneca Ab New compounds
WO2002070523A1 (en) * 2001-03-07 2002-09-12 Pfizer Products Inc. Modulators of chemokine receptor activity
MXPA05001726A (en) * 2002-08-14 2005-05-27 Abbott Lab Azabicyclic compounds are central nervous system active agents.
US7288562B2 (en) 2002-08-23 2007-10-30 Ranbaxy Laboratories Limited Fluoro and sulphonylamino containing 3,6-disubstituted azabicyclo (3.1.0) hexane derivatives as muscarinic receptor antagonists
US7232835B2 (en) * 2002-12-10 2007-06-19 Ranbaxy Laboratories Limited 3,6-Disubstituted azabicyclo derivatives as muscarinic receptor antagonists
FR2866647B1 (en) * 2004-02-20 2006-10-27 Servier Lab NOVEL AZABICYCLIC DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
RU2006146608A (en) 2004-06-09 2008-07-20 Ф.Хоффманн-Ля Рош Аг (Ch) OCTAGHYDROPYRROLO [3,4-c]-DERIVATIVES AND THEIR APPLICATION AS ANTIVIRAL AGENTS
GB0507602D0 (en) * 2005-04-14 2005-05-18 Glaxo Group Ltd Compounds
US7665658B2 (en) 2005-06-07 2010-02-23 First Data Corporation Dynamic aggregation of payment transactions
EP1849771A1 (en) * 2006-04-28 2007-10-31 Laboratorios Del Dr. Esteve, S.A. Bicyclic tetrahydropyrrole compounds
WO2007128458A1 (en) 2006-04-28 2007-11-15 Laboratorios Del Dr. Esteve, S.A. Bicyclic tetrahydropyrrole compounds
EP1849772A1 (en) * 2006-04-28 2007-10-31 Laboratorios Del Dr. Esteve, S.A. Bicyclic tetrahydropyrrole compounds
GB0625198D0 (en) 2006-12-18 2007-01-24 Glaxo Group Ltd Chemical compounds
GB0809479D0 (en) * 2008-05-23 2008-07-02 Glaxo Group Ltd Novel compounds
WO2011140425A1 (en) 2010-05-06 2011-11-10 Vertex Pharmaceuticals Incorporated Heterocyclic chromene-spirocyclic piperidine amides as modulators of ion channels
US9133116B2 (en) 2010-09-28 2015-09-15 Panacea Biotec Ltd. Bicyclic compounds
EP2642998B1 (en) 2010-11-24 2020-09-16 The Trustees of Columbia University in the City of New York A non-retinoid rbp4 antagonist for treatment of age-related macular degeneration and stargardt disease
CN106008504A (en) 2011-02-02 2016-10-12 沃泰克斯药物股份有限公司 Pyrrolopyrazine-spirocyclic piperidine amides as modulators of ion channels
CA2827311A1 (en) 2011-02-18 2012-08-23 Vertex Pharmaceuticals Incorporated Chroman-spirocyclic piperidine amides as modulators of ion channels
AU2012229187B2 (en) 2011-03-14 2016-11-10 Vertex Pharmaceuticals Incorporated Morpholine-spirocyclic piperidine amides as modulators of ion channels
WO2013166037A1 (en) 2012-05-01 2013-11-07 The Trustees Of Columbia University In The City Of New York Non-retinoid antagonists for treatment of eye disorders
WO2014151959A1 (en) 2013-03-14 2014-09-25 The Trustees Of Columbia University In The City Of New York N-alkyl-2-phenoxyethanamines, their preparation and use
WO2014151936A1 (en) 2013-03-14 2014-09-25 The Trustees Of Columbia University In The City Of New York Octahydropyrrolopyrroles, their preparation and use
WO2014152013A1 (en) 2013-03-14 2014-09-25 The Trustees Of Columbia University In The City Of New York 4-phenylpiperidines, their preparation and use
EP2968303B1 (en) 2013-03-14 2018-07-04 The Trustees of Columbia University in the City of New York Octahydrocyclopentapyrroles, their preparation and use
AR097794A1 (en) 2013-09-26 2016-04-13 Mnemosyne Pharmaceuticals Inc OCTAHIDRO-CICLOPENTA MODULATORS [C] NR2B NEGATIVE PIRROL
AU2015253232B2 (en) 2014-04-30 2020-10-01 The Trustees Of Columbia University In The City Of New York Substituted 4-phenylpiperidines, their preparation and use
JO3579B1 (en) 2014-09-26 2020-07-05 Luc Therapeutics Inc N-alkylaryl-5-oxyaryl- octahydro-cyclopenta[c]pyrrole negative allosteric modulators of nr2b
DK3331886T3 (en) * 2015-08-05 2020-08-24 Indivior Uk Ltd DOPAMIN-D3 RECEPTOR ANTAGONISTS WITH A BICYCLO PART
US10870660B2 (en) 2016-07-28 2020-12-22 Shionogi & Co., Ltd. Nitrogen-containing condensed ring compounds having dopamine D3 antagonistic effect
MX2020007849A (en) 2018-01-26 2020-09-25 Shionogi & Co Condensed cyclic compound having dopamine d3 receptor antagonism.
BR112020015712A2 (en) 2018-02-05 2020-12-08 Alkermes, Inc. PAIN TREATMENT COMPOUNDS
BR112021009211A2 (en) 2018-11-14 2021-08-03 Janssen Pharmaceutica N.V. improved synthetic methods of producing fused heterocyclic compounds as orexin receptor modulators
WO2020243423A1 (en) 2019-05-31 2020-12-03 Ikena Oncology, Inc. Tead inhibitors and uses thereof
CA3142351A1 (en) 2019-05-31 2020-12-03 Ikena Oncology, Inc. Tead inhibitors and uses thereof
CN114957087A (en) * 2022-04-13 2022-08-30 湖南复瑞生物医药技术有限责任公司 Preparation method of intermediate of palovaried

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NL110185C (en) * 1958-04-22
NO154582C (en) * 1978-10-20 1986-11-05 Ferrosan Ab ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ACTIVE DIPHENYL-DIBUTYLPIPERAZINE CARBOXAMIDS.
US4435419A (en) * 1981-07-01 1984-03-06 American Cyanamid Company Method of treating depression using azabicyclohexanes
US4605655A (en) * 1984-03-06 1986-08-12 Bristol-Myers Company Antipsychotic 1-fluorophenylbutyl-4-(2-pyrimidinyl)piperazine derivatives
ATE44528T1 (en) * 1984-12-21 1989-07-15 Duphar Int Res MEDICATIONS WITH ANTIPSYCHOTIC EFFECTS.
US4994460A (en) * 1989-06-01 1991-02-19 Bristol-Myers Squibb Co. Agents for treatment of brain ischemia
US5055470A (en) * 1989-06-01 1991-10-08 Bristol-Myers Squibb Co. Method of treatment of ischemia in brain
DE4112353A1 (en) * 1991-04-16 1992-10-22 Basf Ag 1,3,4-TRISUBSTITUTED PIPERIDINE DERIVATIVES, THEIR PRODUCTION AND USE
US5216018A (en) * 1992-02-14 1993-06-01 Du Pont Merck Pharmaceutical Company Hydroisoindolines and hydroisoquinolines as psychotropic
US5532243A (en) * 1992-02-14 1996-07-02 The Dupont Merck Pharmaceutical Company Antipsychotic nitrogen-containing bicyclic compounds
DE4219973A1 (en) * 1992-06-19 1993-12-23 Basf Ag N-substituted azabicycloheptane derivatives, their preparation and use
DE4243287A1 (en) * 1992-06-19 1993-12-23 Basf Ag N-substituted azabicycloheptane derivatives, their preparation and use

Also Published As

Publication number Publication date
DE69425273D1 (en) 2000-08-17
NO306346B1 (en) 1999-10-25
EP0731802B1 (en) 2000-07-12
ATE194620T1 (en) 2000-07-15
FI113644B (en) 2004-05-31
JPH09506346A (en) 1997-06-24
FI962324A0 (en) 1996-06-03
AU680583B2 (en) 1997-07-31
AU1240395A (en) 1995-06-19
NO962286D0 (en) 1996-06-03
EP0731802A1 (en) 1996-09-18
IL111861A0 (en) 1995-03-15
JP3935201B2 (en) 2007-06-20
DE4341403A1 (en) 1995-06-08
BR9408246A (en) 1997-05-27
TW285667B (en) 1996-09-11
IL111861A (en) 1999-08-17
US5703091A (en) 1997-12-30
NO962286L (en) 1996-06-03
FI962324L (en) 1996-06-03
WO1995015327A1 (en) 1995-06-08
DE69425273T2 (en) 2001-01-18

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